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PROCESS FOR OBTAINING ENANTIOMERS AND NON-CREAM MIXTURES OF THE ENANTIOMERS OF N- (2,6-DIMETHYLPHENYL) -1-PROPYL-2-PIPERIDINOCARBOXYL ACID AMIDE; Non-radical mixtures and pharmaceutical compositions containing them.
PROCESS FOR OBTAINING ENANTIOMERS AND NON-CREAM MIXTURES OF THE ENANTIOMERS OF N- (2,6-DIMETHYLPHENYL) -1-PROPYL-2-PIPERIDINOCARBOXYL ACID AMIDE; Non-radical mixtures and pharmaceutical compositions containing them.
The present invention describes a method of separation of the enantiomers of N-(2,6-dimethylphenyl)-1-propyl-2-piperidinocarboxamide. Another object of the present invention refers to the enantiomeric manipulation of the enantiomers of N-(2,6-dimethylphenyl)-1-propyl-2-piperidinocarboxamide, in order to achiever compounds and pharmaceutical compositions presenting diverse enantiomeric excesses of (S)-N-(2,6-dimethylphenyl)-1-propyl-2-piperidinocarboxamide, in order to quantify and determine the participation of (R)-N-(2,6-dimethylphenyl)-1-propyl-2-piperidinocarboxamide in the anesthetic and cardiotoxic effects. These compounds and compositions enantiomerically manipulated demonstrate to present a significant improvement in itsanesthetic properties, presenting a cardiotoxic profile equivalent to pure enantiomer, a (S)-N-(2,6-dimethylphenyl)-1-propyl-2-piperidinocarboxamide.
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